Tuning the electrochemical swelling of polyelectrolyte multilayers toward nanoactuation.

We discuss physicochemical determinants of electrochemical polyelectrolyte multilayer swelling that are relevant to actuator usage. We used electrochemical quartz crystal microbalance with dissipation monitoring (EC-QCM-D) and cyclic voltammetry to compare the electrochemical swelling of two types of ferrocyanide-containing polyelectrolyte multilayers, poly(l-glutamic acid)/poly(allylamine hydrochloride) (PGA/PAH), and carboxymethyl cellulose/poly(diallyldimethylammonium chloride) (CMC/PDDA). We showed that ferrocyanide oxidation causes the swelling of PGA/PAH multilayers whereas it results in the contraction of CMC/PDDA multilayers. This behavior can be attributed to the presence of a positive and a negative Donnan potential in the case of PGA/PAH and CMC/PDDA multilayers, respectively. Using multilayers consisting of PGA and poly(allylamine) ferrocene (PGA/PAH-FC), we applied EC-QCM-D and demonstrated potentiostatic thickness control with nanometer precision and showed that the multilayer's thickness depends linearly on the applied potential within a certain potential range.

The entropy of water in swelling PGA/PAH polyelectrolyte multilayers.

We investigated the thermodynamical properties of water exchanged in poly(l-glutamic acid)/poly(allylamine)hydrochloride (PGA/PAH) polyelectrolyte multilayers containing ferrocyanide. Oxidation/reduction of the ferrocyanide in the multilayer caused a reversible swelling/contraction of the film due to the uptake/release of counter ions and water. We used electrochemical quartz crystal microbalance and electrochemical microcalorimetry to correlate the amount of water with the accompanying entropy changes during electrochemical swelling of the multilayer for a series of different anions at different concentrations. The number of exchanged water molecules was highly dependent on the ionic strength and the type of anion in the buffer solution. However, the entropy change per exchanged water molecule was found to be independent of these two parameters. The water molecules in the polyelectrolyte multilayer have reduced the entropy compared to that of bulk water (≈-1 J mol(-1) K(-1)). A comparison of hydration entropies for free polyelectrolytes and PGA/PAH multilayers suggests that such systems are mainly stabilized by water release during multilayer construction.

Electrochemical crystallization of plasmonic nanostructures.

We show how gold recrystallizes when under the influence of electrochemical potentials. This "cold annealing" occurs without charge transfer reactions and preserves nanoscale structural features. By performing the process on plasmonic nanostructures, grain growth is monitored noninvasively by optical spectroscopy. In this way, the influence from crystal structure on plasmon resonances can be investigated independently. Observed spectral changes are in excellent agreement with analytical models and changes in electron relaxation time and plasma frequency are calculated.

Electrical microcurrent to prevent conditioning film and bacterial adhesion to urological stents.

Long-term catheters remain a significant clinical problem in urology due to the high rate of bacterial colonization, infection, and encrustation. Minutes after insertion of a catheter, depositions of host urinary components onto the catheter surface form a conditioning film actively supporting the bacterial adhesion process. We investigated the possibility of reducing or avoiding the buildup of these naturally forming conditioning films and of preventing bacterial adhesion by applying different current densities to platinum electrodes as a possible catheter coating material. In this model we employed a defined environment using artificial urine and Proteus mirabilis. The film formation and desorption was analyzed by highly mass sensitive quartz crystal microbalance and surface sensitive atomic force microscopy. Further, we performed bacterial staining to assess adherence, growth, and survival on the electrodes with different current densities. By applying alternating microcurrent densities on platinum electrodes, we could produce a self regenerative surface which actively removed the conditioning film and significantly reduced bacterial adherence, growth, and survival. The results of this study could easily be adapted to a catheter design for clinical use.

Improving Ionic Conductivity and Lithium-Ion Transference Number in Lithium-Ion Battery Separators.

The microstructure of lithium-ion battery separators plays an important role in separator performance; however, here we show that a geometrical analysis falls short in predicting the lithium-ion transport in the electrolyte-filled pore space. By systematically modifying the surface chemistry of a commercial polyethylene separator while keeping its microstructure unchanged, we demonstrate that surface chemistry, which alters separator-electrolyte interactions, influences ionic conductivity and lithium-ion transference number. Changes in separator surface chemistry, particularly those that increase lithium-ion transference numbers can reduce voltage drops across the separator and improve C-rate capability.

A physical model describing the interaction of nuclear transport receptors with FG nucleoporin domain assemblies.

The permeability barrier of nuclear pore complexes (NPCs) controls bulk nucleocytoplasmic exchange. It consists of nucleoporin domains rich in phenylalanine-glycine motifs (FG domains). As a bottom-up nanoscale model for the permeability barrier, we have used planar films produced with three different end-grafted FG domains, and quantitatively analyzed the binding of two different nuclear transport receptors (NTRs), NTF2 and Importin ß, together with the concomitant film thickness changes. NTR binding caused only moderate changes in film thickness; the binding isotherms showed negative cooperativity and could all be mapped onto a single master curve. This universal NTR binding behavior - a key element for the transport selectivity of the NPC - was quantitatively reproduced by a physical model that treats FG domains as regular, flexible polymers, and NTRs as spherical colloids with a homogeneous surface, ignoring the detailed arrangement of interaction sites along FG domains and on the NTR surface.

Nanoplasmonic sensing of metal-halide complex formation and the electric double layer capacitor.

Many nanotechnological devices are based on implementing electrochemistry with plasmonic nanostructures, but these systems are challenging to understand. We present a detailed study of the influence of electrochemical potentials on plasmon resonances, in the absence of surface coatings and redox active molecules, by synchronized voltammetry and spectroscopy. The experiments are performed on gold nanodisks and nanohole arrays in thin gold films, which are fabricated by improved methods. New insights are provided by high resolution spectroscopy and variable scan rates. Furthermore, we introduce new analytical models in order to understand the spectral changes quantitatively. In contrast to most previous literature, we find that the plasmonic signal is caused almost entirely by the formation of ionic complexes on the metal surface, most likely gold chloride in this study. The refractometric sensing effect from the ions in the electric double layer can be fully neglected, and the charging of the metal gives a surprisingly small effect for these systems. Our conclusions are consistent for both localized nanoparticle plasmons and propagating surface plasmons. We consider the results in this work especially important in the context of combined electrochemical and optical sensors.

Ion-induced cell sheet detachment from standard cell culture surfaces coated with polyelectrolytes.

Polyelectrolyte multilayers (PEMs), formed by alternating layer-by-layer deposition of polyanions and polycations, are an ideal substrate for controlling cellular adhesion and behavior. In the present study we propose a simple mechanism for the controlled detachment of C(2)C(12) myoblasts cell sheets from PEMs consisting of poly(l-lysine) and hyaluronic acid with a topmost layer of fibronectin. The multilayers were deposited on two standard cell culture surfaces: glass and polystyrene. Adding a low concentration of nontoxic ferrocyanide to the cell culture medium resulted in erosion of the polyelectrolyte multilayer and rapid detachment of viable cell sheets. Additional Quartz Crystal Microbalance and Atomic Force Microscopy measurements indicated that the detached cells retained their extracellular matrix and that no polyelectrolyte molecules remained bound to the cell sheets. The dissolution of polyelectrolyte multilayers by multivalent ions is a promising approach to cell sheet engineering that could potentially be used for regenerative medicine.

Ion and solvent exchange processes in PGA/PAH polyelectrolyte multilayers containing ferrocyanide.

We investigated ion exchange processes in poly(L-glutamic acid)/poly(allylamine)hydrochloride (PGA/PAH) polyelectrolyte multilayers containing ferrocyanide using electrochemical quartz crystal microbalance and infrared spectroscopy in attenuated total reflection. Oxidation/reduction of the ferrocyanide caused a reversible swelling of the film. We showed that the electrochemical swelling of this multilayer system depends on the ionic properties of the contacting buffer. A model was developed to explain the influence of ionic strength, the pH value, and the charge of the counterions in the buffer on the swelling behavior, by relating the swelling of the multilayer to the exchange of counterions and water molecules between the buffer and the multilayer. Changing the salts in the buffer, while maintaining the same ionic strength, showed that the swelling of the multilayer is related to the counterions' molecular mass, hydration properties, and binding strength to PAH. The hydration efficiency of different monovalent anions follows the Hofmeister series, decreasing from kosmotropic ions to chaotropic ones. In contrast, the strong binding affinity of divalent anions causes them to diverge from the Hofmeister series and to release ferrocyanide from the multilayer.

Engineering the extracellular environment: Strategies for building 2D and 3D cellular structures.

Cell fate is regulated by extracellular environmental signals. Receptor specific interaction of the cell with proteins, glycans, soluble factors as well as neighboring cells can steer cells towards proliferation, differentiation, apoptosis or migration. In this review, approaches to build cellular structures by engineering aspects of the extracellular environment are described. These methods include non-specific modifications to control the wettability and stiffness of surfaces using self-assembled monolayers (SAMs) and polyelectrolyte multilayers (PEMs) as well as methods where the temporal activation and spatial distribution of adhesion ligands is controlled. Building on these techniques, construction of two-dimensional cell sheets using temperature sensitive polymers or electrochemical dissolution is described together with current applications of these grafts in the clinical arena. Finally, methods to pattern cells in three-dimensions as well as to functionalize the 3D environment with biologic motifs take us one step closer to being able to engineer multicellular tissues and organs.